Canonical Allele Identifier: CA134569

Gene: NRAS

Linked Data

• ClinVar Variation Id: 40476
• ClinVar RCV Id: RCV000037577 ; RCV000587570 ; RCV001100796 ; RCV001080827 ; RCV001813240 ; RCV002453281
• dbSNP Id: rs143020946
• ExAC: 1:115252280 C / T
• gnomAD v2: 1-115252280-C-T
• gnomAD v3: 1-114709659-C-T
• gnomAD v4: 1-114709659-C-T
• MyVariant Identifiers: chr1:g.115252280C>T (hg19) ; chr1:g.114709659C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.114709659C>T , CM000663.2:g.114709659C>T	GRCh38
NC_000001.10:g.115252280C>T , CM000663.1:g.115252280C>T	GRCh37
NC_000001.9:g.115053803C>T	NCBI36
NG_007572.1:g.12236G>A , LRG_92:g.12236G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000369535.5:c.360G>A MANE Select	ENSP00000358548.4:p.Leu120=
ENST00000369535.4:c.360G>A	ENSP00000358548.4:p.Leu120=
NM_002524.4:c.360G>A	NP_002515.1:p.Leu120=
NM_002524.5:c.360G>A MANE Select	NP_002515.1:p.Leu120=